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  2. L1 syndrome - Wikipedia

    en.wikipedia.org/wiki/L1_syndrome

    L1 syndrome is a group of mild to severe X-linked recessive disorders that share a common genetic basis. The spectrum of L1 syndrome disorders includes X-linked complicated corpus callosum dysgenesis, spastic paraplegia 1, MASA syndrome, and X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS).

  3. Spina bifida - Wikipedia

    en.wikipedia.org/wiki/Spina_bifida

    Spina bifida (SB; /ˌspaɪnə ˈbɪfɪdə/, [9] Latin for 'split spine') [10] is a birth defect in which there is incomplete closing of the spine and the membranes around the spinal cord during early development in pregnancy. [1] There are three main types: spina bifida occulta, meningocele and myelomeningocele. [1]

  4. Lateral meningocele syndrome - Wikipedia

    en.wikipedia.org/wiki/Lateral_meningocele_syndrome

    This genetic disease in very rare. There have been 16 reported cases in 14 different families. [4] 9 cases were male patients and 7 cases were female patients. [4] Inheritance of Lehman syndrome from a parent has occurred. However de novo mutations of the Notch 3 gene are more common. [4] There is no prevalence in specific populations. [5]

  5. Encephalocele - Wikipedia

    en.wikipedia.org/wiki/Encephalocele

    Encephaloceles are often accompanied by craniofacial abnormalities or other brain malformations. Symptoms may include neurologic problems, hydrocephalus (cerebrospinal fluid accumulated in the brain), spastic quadriplegia (paralysis of the limbs), microcephaly (an abnormally small head), ataxia (uncoordinated muscle movement), developmental delay, vision problems, mental and growth retardation ...

  6. Neural tube defect - Wikipedia

    en.wikipedia.org/wiki/Neural_tube_defect

    Neural tube defects (NTDs) are a group of birth defects in which an opening in the spine or cranium remains from early in human development. In the third week of pregnancy called gastrulation, specialized cells on the dorsal side of the embryo begin to change shape and form the neural tube.

  7. Colpocephaly - Wikipedia

    en.wikipedia.org/wiki/Colpocephaly

    Hydrocephalus; schizencephaly; microgyria; microcephaly; Pierre-Robin syndrome; Neurofibromatosis; Often colpocephaly occurs as a result of hydrocephalus. Hydrocephalus is the accumulation of cerebrospinal fluid (CSF) in the ventricles or in the subarachnoid space over the brain. The increased pressure due to this condition dilates occipital ...

  8. Aqueductal stenosis - Wikipedia

    en.wikipedia.org/wiki/Aqueductal_stenosis

    Blockage of the aqueduct can lead to hydrocephalus, specifically as a common cause of congenital and/or obstructive hydrocephalus. [ 1 ] [ 2 ] The aqueduct of Sylvius is the channel which connects the third ventricle to the fourth ventricle and is the narrowest part of the CSF pathway with a mean cross-sectional area of 0.5 mm 2 in children and ...

  9. Mucopolysaccharidosis - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis

    Neurological symptoms may include mild to moderate intellectual disability by age 3, communicating hydrocephalus, nerve entrapment, corneal clouding, and some loss of peripheral and night vision. Other symptoms include short stature, some skeletal irregularities, joint stiffness and restricted movement, and umbilical and/or inguinal hernias.